AbstractIn the mid-twentieth century (1948–57), North America experienced a severe drought forced by cold tropical Pacific sea surface temperatures (SSTs). If these SSTs recurred, it would likely cause another drought, but in a world substantially warmer than the one in which the original event took place. We use a 20-member ensemble of the GISS climate model to investigate the drought impacts of a repetition of the mid-twentieth-century SST anomalies in a significantly warmer world. Using observed SSTs and mid-twentieth-century forcings (Hist-DRGHT), the ensemble reproduces the observed precipitation deficits during the cold season (October–March) across the Southwest, southern plains, and Mexico and during the warm season (April–September) in the southern plains and the Southeast. Under analogous SST forcing and enhanced warming (Fut-DRGHT, ≈3 K above preindustrial), cold season precipitation deficits are ameliorated in the Southwest and southern plains and intensified in the Southeast, whereas during the warm season precipitation deficits are enhanced across North America. This occurs primarily from greenhouse gas–forced trends in mean precipitation, rather than changes in SST teleconnections. Cold season runoff deficits in Fut-DRGHT are significantly amplified over the Southeast, but otherwise similar to Hist-DRGHT over the Southwest and southern plains. In the warm season, however, runoff and soil moisture deficits during Fut-DRGHT are significantly amplified across the southern United States, a consequence of enhanced precipitation deficits and increased evaporative losses due to warming. Our study highlights how internal variability and greenhouse gas–forced trends in hydroclimate are likely to interact over North America, including how changes in both precipitation and evaporative demand will affect future drought.

Biophysical vegetation responses to elevated atmospheric carbon dioxide (CO₂) affect regional hydroclimate through two competing mechanisms. Higher CO₂ increases leaf area (LAI), thereby increasing transpiration and water losses. Simultaneously, elevated CO₂ reduces stomatal conductance and transpiration, thereby increasing rootzone soil moisture. Which mechanism dominates in the future is highly uncertain, partly because these two processes are difficult to explicitly separate within dynamic vegetation models. We address this challenge by using the GISS ModelE global climate model to conduct a novel set of idealized 2×CO₂ sensitivity experiments to: evaluate the total vegetation biophysical contribution to regional climate change under high CO₂; and quantify the separate contributions of enhanced LAI and reduced stomatal conductance to regional hydroclimate responses. We find that increased LAI exacerbates soil moisture deficits across the sub-tropics and more water-limited regions, but also attenuates warming by ∼0.5-1°C in the US Southwest, Central Asia, Southeast Asia, and northern South America. Reduced stomatal conductance effects contribute ∼1°C of summertime warming. For some regions, enhanced LAI and reduced stomatal conductance produce nonlinear and either competing or mutually amplifying hydroclimate responses. In northeastern Australia, these effects combine to exacerbate radiation-forced warming and contribute to year-round water limitation. Conversely, at higher latitudes these combined effects result in less warming than would otherwise be predicted due to nonlinear responses. These results highlight substantial regional variation in CO₂-driven vegetation responses and the importance of improving model representations of these processes to better quantify regional hydroclimate impacts.

Spatially diverse trends in population growth, climate change, industrialization, urbanization and economic development are expected to change future food supply and demand. These changes may affect the suitability of land for food production, implying elevated risks especially for resourceconstrained, food-importing countries.Wepresent the evolution of biophysical redundancy for agricultural production at country level, from 1992 to 2012. Biophysical redundancy, defined as unused biotic and abiotic environmental resources, is represented by the potential food production of 'spare land', available water resources (i.e., not already used for human activities), as well as production increases through yield gap closure on cultivated areas and potential agricultural areas. In 2012, the biophysical redundancy of 75 (48) countries, mainly in North Africa, Western Europe, the Middle East and Asia, was insufficient to produce the caloric nutritional needs for at least 50% (25%) of their population during a year. Biophysical redundancy has decreased in the last two decades in 102 out of 155 countries, 11 of these went from high to limited redundancy, and nine of these from limited to very low redundancy. Although the variability of the drivers of change across different countries is high, improvements in yield and population growth have a clear impact on the decreases of redundancy towards the very low redundancy category.Wetook a more detailed look at countries classified as 'Low Income Economies (LIEs)' since they are particularly vulnerable to domestic or external food supply changes, due to their limited capacity to offset for food supply decreases with higher purchasing power on the international market. Currently, nine LIEs have limited or very low biophysical redundancy. Many of these showed a decrease in redundancy over the last two decades, which is not always linked with improvements in per capita food availability.